| Autor: |
Stipniece L; Rudolfs Cimdins Riga Biomaterials Innovations and Development Centre, Riga Technical University, LV-1007 Riga, Latvia.; Baltic Biomaterials Centre of Excellence, Headquarters at Riga Technical University, LV-1048 Riga, Latvia., Rezevska D; Department of Biology and Microbiology, Riga Stradins University, LV-1048 Riga, Latvia.; Joint Laboratory, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia., Kroica J; Department of Biology and Microbiology, Riga Stradins University, LV-1048 Riga, Latvia., Racenis K; Department of Biology and Microbiology, Riga Stradins University, LV-1048 Riga, Latvia.; Centre of Nephrology, Pauls Stradins Clinical University Hospital, LV-1002 Riga, Latvia. |
| Abstrakt: |
The use of implant materials is always associated with the risk of infection. Moreover, the effectiveness of antibiotics is reduced due to antibiotic-resistant pathogens. Thus, selecting the appropriate alternative antimicrobials for local delivery systems is correlated with successful infection management. We evaluated immobilization of the S. aureus specific bacteriophages in clinically recognized biopolymers, i.e., chitosan and alginate, to control the release profile of the antimicrobials. The high-titre S. aureus specific bacteriophages were prepared from commercial bacteriophage cocktails. The polymer mixtures with the propagated bacteriophages were then prepared. The stability of the S. aureus bacteriophages in the biopolymer solutions was assessed. In the case of chitosan, no plaques indicating the presence of the lytic bacteriophages were observed. The titre reduction of the S. aureus bacteriophages in the Na-alginate was below 1 log unit. Furthermore, the bacteriophages retained their lytic activity in the alginate after crosslinking with Ca 2+ ions. The release of the lytic S. aureus bacteriophages from the Ca-alginate matrices in the TRIS-HCl buffer solution (pH 7.4 ± 0.2) was determined. After 72 h-0.292 ± 0.021% of bacteriophages from the Ca-alginate matrices were released. Thus, sustained release of the lytic S. aureus bacteriophages can be ensured. |
